Precision For Medicine

Medical Director

Precision For Medicine

full-time

Posted on:

Location Type: Remote

Location: United States

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Salary

💰 $227,600 - $341,400 per year

Job Level

About the role

  • Serve as the project physician and provide medical and scientific expertise to project teams
  • Ensure the accuracy and integrity of the data resulting from the trial, with concentrated focus on patient safety
  • Participate in the strategic planning and execution of critical development programs for a variety of clients in oncology or autoimmune disease
  • Support Business Development and Proposals teams by participating in the RFP process; prepare medical considerations section for proposals; and support or participate in bid defense meetings
  • Write or edit scientific content of deliverables within budget and timelines
  • Collaborate with Regulatory Affairs on regulatory product landscape and strategies as a part of overall drug development strategy
  • Provide scientific insight and create content for specified company releases (e.g., white papers and publication manuscripts)
  • Review and revise protocols, case report forms, training materials, project specific tools, analysis plans, study designs, clinical trial reports and new drug applications
  • Review laboratory values, adverse events, coded adverse event and medication data, and data tables, listings and figures as needed
  • Serve as a medical resource for study sites, the project team and clients
  • Assist in the preparation of the Medical Monitoring Plan and materials for investigator meetings and staff training sessions
  • Assume responsibility for medical and safety monitoring on assigned projects
  • Participate in feasibility discussions relating to specific project proposals
  • Develop training modules and provide training concentrating on disease states
  • Participate in process improvement activities
  • Collaborate with Senior Vice President, Global Medical and other members of the Medical Science Department to support growth and development activities globally

Requirements

  • MD, DO, MBBS, or equivalent medical qualifications
  • 5+ years of clinical experience
  • Completed an accredited medical residency program
  • Completed a fellowship or equivalent relevant to assigned programs (e.g., oncology and/or hematology; rheumatology; allergy & immunology; endocrinology; gastroenterology; nephrology; neurology; or other related subspecialty)
  • 5+ years of experience in oncology or autoimmune disease clinical research (depending on client and/or program assignment)
  • Demonstrated expertise across the lifecycle of oncology or autoimmune disease drug development, with ability to strategically analyze clinical trial protocols in the assigned therapeutic area
  • Availability for domestic and international travel including overnight stays (approximate 30% travel requirement)
Benefits
  • Health insurance
  • Retirement savings benefits
  • Life insurance
  • Disability benefits
  • Parental leave
  • Paid time off for sick leave and vacation
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
clinical researchmedical writingdata analysisprotocol reviewcase report form reviewadverse event reviewmedical monitoringtraining module developmentstrategic planningdrug development
Soft Skills
collaborationcommunicationleadershiporganizational skillsproblem-solvingattention to detailproject managementstrategic analysistraining and mentoringclient engagement
Certifications
MDDOMBBSmedical residencyfellowship in oncologyfellowship in hematologyfellowship in rheumatologyfellowship in allergy & immunologyfellowship in endocrinologyfellowship in gastroenterology